Ethyl(trimethyl)silane

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Reagent Code: #180851
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CAS Number 3439-38-1

science Other reagents with same CAS 3439-38-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 102.25 g/mol
Formula C₅H₁₄Si
thermostat Physical Properties
Boiling Point 58.7 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Ethyl(trimethyl)silane is an organosilicon compound primarily used as a reference standard in nuclear magnetic resonance (NMR) spectroscopy, especially for 29Si NMR, due to its characteristic chemical shift. It also serves as an internal standard in gas chromatography (GC) for calibration purposes. In organic synthesis, it acts as a building block for more complex silicon-containing molecules, often via transition-metal-catalyzed cross-coupling reactions or C-H activation methods. Additionally, it is employed in materials science for surface modification of substrates to introduce hydrophobic characteristics, and in the study of silicon-carbon bond properties.

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inventory 1g
10-20 days ฿9,200.00

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Ethyl(trimethyl)silane
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Ethyl(trimethyl)silane is an organosilicon compound primarily used as a reference standard in nuclear magnetic resonance (NMR) spectroscopy, especially for 29Si NMR, due to its characteristic chemical shift. It also serves as an internal standard in gas chromatography (GC) for calibration purposes. In organic synthesis, it acts as a building block for more complex silicon-containing molecules, often via transition-metal-catalyzed cross-coupling reactions or C-H activation methods. Additionally, i
Ethyl(trimethyl)silane is an organosilicon compound primarily used as a reference standard in nuclear magnetic resonance (NMR) spectroscopy, especially for 29Si NMR, due to its characteristic chemical shift. It also serves as an internal standard in gas chromatography (GC) for calibration purposes. In organic synthesis, it acts as a building block for more complex silicon-containing molecules, often via transition-metal-catalyzed cross-coupling reactions or C-H activation methods. Additionally, it is employed in materials science for surface modification of substrates to introduce hydrophobic characteristics, and in the study of silicon-carbon bond properties.
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